Enable job alerts via email!

Qualified Person - Pharmaceuticals

Smart4Sciences

England

On-site

GBP 45,000 - 75,000

Full time

20 days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player is seeking a Qualified Person to ensure the release of pharmaceutical products in compliance with regulations. This role involves reviewing batch records, certifying products, and overseeing quality assurance processes. The ideal candidate will have a strong background in small molecule manufacturing and a thorough understanding of GMP and regulatory requirements. This is an urgent opportunity with immediate interviews available, making it a perfect chance for qualified professionals to make a significant impact in the pharmaceutical sector.

Qualifications

  • Eligible to act as Qualified Person in the UK with extensive experience in GxP.
  • Strong understanding of small molecule manufacturing and solid oral dosage forms.

Responsibilities

  • Perform QP batch certification and provide support for quality issues.
  • Approve Finished Product for release and coordinate inspections.

Skills

GMP Compliance
Quality Assurance
Pharmaceutical Manufacturing
Regulatory Knowledge
Batch Certification

Education

Qualified Person Eligibility in UK
Experience in Pharmaceutical Industry

Job description

Smart4Sciences are currently working with a Pharmaceutical Company in the north of England to recruit a Qualified Person responsible for sign off and release of finished Pharmaceutical products.


As a QP you will be responsible for reviewing and evaluating batch records and performing batch certification and release of solid-dose products in accordance with GMP and the Human Medicines Regulations.


Key Responsibilities
  1. Performing QP batch certification of licensed medicines (per applicable regulations) and providing QP support as required for Quality issues.
  2. To act as 'Qualified Person' in approving Finished Product for release onto the marketplace.
  3. Verify and ensure that the products are manufactured, packed and tested to the requirements of registered MA.
  4. Responsible as named QP on the site MIA. To coordinate the preparation and hosting of MHRA and customer inspections.
Key Requirements
  1. Eligible to act as Qualified person in UK.
  2. Strong understanding of small molecule manufacturing with direct experience in solid oral dosage forms.
  3. Extensive Pharmaceutical Industry with hands-on experience in development/quality in a GxP environment.
  4. Knowledge and understanding of drug development process and the Global Regulatory Requirements and regulations related to GxP.
  5. Excellent working knowledge of EU GMPs, especially in the interpretation of requirements and guidance for the development, manufacture, control, and distribution of commercial product.

This Qualified Person vacancy is an urgent requirement with interviews happening now - if you would be interested please apply today.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.